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韩国采用串联质谱法对新生儿和高危儿童群体进行先天性代谢疾病筛查:三年报告

Screening of newborns and high-risk group of children for inborn metabolic disorders using tandem mass spectrometry in South Korea: a three-year report.

作者信息

Yoon Hye-Ran, Lee Kyung Ryul, Kang Seungwoo, Lee Dong Hwan, Yoo Han-Wook, Min Won-Ki, Cho Dong Hee, Shin Son Moon, Kim Jongwon, Song Junghan, Yoon Ho Joo, Seo Sonsang, Hahn Si Houn

机构信息

Department of Biochemical Genetics, Seoul Clinical Laboratories, Seoul Medical Science Institute, 7-14 Dongbinggo-dong Yongsan-gu, Seoul, 140-809, Republic of Korea.

出版信息

Clin Chim Acta. 2005 Apr;354(1-2):167-80. doi: 10.1016/j.cccn.2004.11.032.

Abstract

BACKGROUND

Mass screening using tandem mass spectrometry(MS/MS) was initiated to determine if the incidence of metabolic disorder is sufficiently high to meet the criteria for newborn screening, and whether or not early medical intervention might be beneficial to the patients.

METHODS

Newborns and children in a high-risk group were screened using MS/MS from April 2001 to March 2004. Blood spots of newborns were collected between 48 and 72 h after birth. The dried blood spots was extracted with 150 microl of methanol, and analyzed by MS/MS.

RESULTS

From April 2001 to March 2004, 79,179 newborns were screened for organic, amino and fatty acid metabolism disorders, which account for approximately 5.4% of annual births in South Korea. Twenty-eight newborns were diagnosed with one of the metabolic disorders and the collective estimated prevalence amounted to 1 in 2800 with a sensitivity of 97.67%, a specificity of 99.28%, a recall rate of 0.05%, and a positive predictive value of 6.38%. 6795 infants/children at high risk were screened and 20 were confirmed to have metabolic disorders.

CONCLUSION

The collective total prevalence of 1:2800 in newborns indicates an underestimation of the incidence of metabolic disorders prior to implementing MS/MS screening in South Korea.

摘要

背景

启动串联质谱(MS/MS)大规模筛查,以确定代谢紊乱的发病率是否足够高,符合新生儿筛查标准,以及早期医学干预是否对患者有益。

方法

2001年4月至2004年3月,对高危组新生儿和儿童进行MS/MS筛查。新生儿出生后48至72小时采集血斑。用150微升甲醇提取干血斑,并通过MS/MS进行分析。

结果

2001年4月至2004年3月,对79179名新生儿进行了有机、氨基酸和脂肪酸代谢紊乱筛查,约占韩国年出生人口的5.4%。28名新生儿被诊断患有其中一种代谢紊乱,总体估计患病率为1/2800,灵敏度为97.67%,特异度为99.28%,召回率为0.05%,阳性预测值为6.38%。对6795名高危婴儿/儿童进行了筛查,20人被确诊患有代谢紊乱。

结论

新生儿总体患病率为1:2800,表明在韩国实施MS/MS筛查之前,代谢紊乱的发病率被低估了。

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